Mitochondrial Genetic Disorders: Cell Signaling and Pharmacological Therapies

Mitochondrial fatty acid oxidation (FAO) and respiratory chain (RC) defects form a large group of inherited monogenic disorders sharing many common clinical and pathophysiological features, including disruption of mitochondrial bioenergetics, but also, for example, oxidative stress and accumulation...

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Detalles Bibliográficos
Autores principales: Djouadi, Fatima, Bastin, Jean
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6523966/
https://www.ncbi.nlm.nih.gov/pubmed/30925787
http://dx.doi.org/10.3390/cells8040289

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6523966/
https://www.ncbi.nlm.nih.gov/pubmed/30925787
http://dx.doi.org/10.3390/cells8040289

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